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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01036048
Other study ID # N28LBCF80-07
Secondary ID
Status Completed
Phase N/A
First received December 7, 2009
Last updated December 18, 2009
Start date May 2009
Est. completion date December 2009

Study information

Verified date December 2009
Source Catholic University of the Sacred Heart
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Observational

Clinical Trial Summary

A meta-analysis to compare outcomes of drug eluting stents (DES) versus bare metal stent (BMS) in saphenous vein graft (SVG) disease.


Description:

To compare outcomes (death, myocardial infarction, target vessel revascularization) of drug eluting stent versus bare metal stent in saphenous vein graft disease.


Recruitment information / eligibility

Status Completed
Enrollment 5806
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- CABG disease

- randomized studies

- not randomized studies

Exclusion Criteria:

- studies reporting composite and not single endpoints, duplicate reporting

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Device:
drug eluting stent
pts with cabg disease treated with drug eluting stent
bare metal stent
pts with cabg disease treated with bare metal stent

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Catholic University of the Sacred Heart

Outcome

Type Measure Description Time frame Safety issue
Primary death years depending from studies retrieved No
Secondary myocardial infarction years depending from study retrieved No
Secondary target vessel revascularization years depending from study retrieved No
See also
  Status Clinical Trial Phase
Completed NCT02053909 - Ticagrelor Antiplatelet Therapy to Reduce Graft Events and Thrombosis Phase 4
Completed NCT00263263 - RRISC Study: Reduction of Restenosis In Saphenous Vein Grafts With Cypher Sirolimus-Eluting Stent. Phase 2
Recruiting NCT03175952 - Virtual Histology Intravascular Ultrasound to Evaluate Prognostic Risks of Saphenous Vein Graft Disease Before Percutaneous Coronary Intervention. N/A
Completed NCT01528709 - Aggressive Cholesterol Therapy to Inhibit Vein Graft Events After CABG (ACTIVE Trial) Phase 3
Completed NCT00453518 - The RETRIEVE Study: Use of the FiberNet® Embolic Protection System in Saphenous Vein Grafts N/A
Terminated NCT00264706 - PolyArginine Treated vEiN grafTs (PATENT) Phase 1/Phase 2
Terminated NCT01042444 - Use of the GARDEX™ Embolic Protection Device During Percutaneous Coronary Interventions of Saphenous Vein Graft N/A